Role of sphingolipids in the pathogenesis of intrahepatic cholestasis

•Intrahepatic cholestasis related perinatal complications include premature birth, meconium-stained amniotic fluid, fetal bradycardia, fetal respiratory distress syndrome and intrauterine fetal demise.•Cholestasis treatment with UDCA is known to be very effective.•Sphingolipids can potentially becom...

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Published inProstaglandins & other lipid mediators Vol. 147; p. 106399
Main Authors Mikucka-Niczyporuk, Agnieszka, Pierzynski, Piotr, Lemancewicz, Adam, Kosinski, Przemyslaw, Charkiewicz, Karol, Knas, Małgorzata, Kacerovsky, Marian, Blachnio-Zabielska, Agnieszka, Laudanski, Piotr
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LanguageEnglish
Published United States Elsevier Inc 01.04.2020
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Abstract •Intrahepatic cholestasis related perinatal complications include premature birth, meconium-stained amniotic fluid, fetal bradycardia, fetal respiratory distress syndrome and intrauterine fetal demise.•Cholestasis treatment with UDCA is known to be very effective.•Sphingolipids can potentially become screening markers as well as markers for monitoring the treatment of ICP in pregnant women. Intrahepatic cholestasis of pregnancy (ICP) is the most common pregnancy-related liver disorder that affects from 0.2% to 15.6% pregnant women. The disease is connected with increased risk of fetal morbidity and mortality, but is unfortunately detected quite late. The diagnosis of ICP is based on only one manifestation: pruritus which mainly affects soles and palms. Twenty intrahepatic cholestasis of pregnancy (ICP) women and twenty healthy pregnant women (control group) took part in the study. In the study group, blood sampling for baseline measurements was performed on the first day of hospital stay – before the commencement of treatment with ursodeoxycholic acid (UDCA) – and repeated after 7 days of 900 mg UDCA per day. An additional blood sample was collected on the second day after childbirth. In the control group, blood samples were collected directly after hospital admission. We compared plasma sphingolipids in samples of the subjects from ICP and ICP + UDCA-treated groups as well as the ICP group after delivery with the healthy controls. Of all sphingolipids, the median values of C16-Cer and C18-Cer were significantly higher in the plasma of cholestasis patients not treated with UDCA as compared to the control. Following 7 days of UDCA treatment, a considerable decrease in C16-Cer, C18-Cer and the total concentration of bile acids was noted as compared to the baseline. It is known that sphingolipids serve as modulators of liver regeneration. We assume these substances could be potential markers for detecting early onsets of intrahepatic cholestasis of pregnancy.
AbstractList Intrahepatic cholestasis of pregnancy (ICP) is the most common pregnancy-related liver disorder that affects from 0.2% to 15.6% pregnant women. The disease is connected with increased risk of fetal morbidity and mortality, but is unfortunately detected quite late. The diagnosis of ICP is based on only one manifestation: pruritus which mainly affects soles and palms. Twenty intrahepatic cholestasis of pregnancy (ICP) women and twenty healthy pregnant women (control group) took part in the study. In the study group, blood sampling for baseline measurements was performed on the first day of hospital stay - before the commencement of treatment with ursodeoxycholic acid (UDCA) - and repeated after 7 days of 900 mg UDCA per day. An additional blood sample was collected on the second day after childbirth. In the control group, blood samples were collected directly after hospital admission. We compared plasma sphingolipids in samples of the subjects from ICP and ICP + UDCA-treated groups as well as the ICP group after delivery with the healthy controls. Of all sphingolipids, the median values of C16-Cer and C18-Cer were significantly higher in the plasma of cholestasis patients not treated with UDCA as compared to the control. Following 7 days of UDCA treatment, a considerable decrease in C16-Cer, C18-Cer and the total concentration of bile acids was noted as compared to the baseline. It is known that sphingolipids serve as modulators of liver regeneration. We assume these substances could be potential markers for detecting early onsets of intrahepatic cholestasis of pregnancy.
Intrahepatic cholestasis of pregnancy (ICP) is the most common pregnancy-related liver disorder that affects from 0.2% to 15.6% pregnant women. The disease is connected with increased risk of fetal morbidity and mortality, but is unfortunately detected quite late. The diagnosis of ICP is based on only one manifestation: pruritus which mainly affects soles and palms.BACKGROUND & AIMSIntrahepatic cholestasis of pregnancy (ICP) is the most common pregnancy-related liver disorder that affects from 0.2% to 15.6% pregnant women. The disease is connected with increased risk of fetal morbidity and mortality, but is unfortunately detected quite late. The diagnosis of ICP is based on only one manifestation: pruritus which mainly affects soles and palms.Twenty intrahepatic cholestasis of pregnancy (ICP) women and twenty healthy pregnant women (control group) took part in the study. In the study group, blood sampling for baseline measurements was performed on the first day of hospital stay - before the commencement of treatment with ursodeoxycholic acid (UDCA) - and repeated after 7 days of 900 mg UDCA per day. An additional blood sample was collected on the second day after childbirth. In the control group, blood samples were collected directly after hospital admission. We compared plasma sphingolipids in samples of the subjects from ICP and ICP + UDCA-treated groups as well as the ICP group after delivery with the healthy controls.METHODSTwenty intrahepatic cholestasis of pregnancy (ICP) women and twenty healthy pregnant women (control group) took part in the study. In the study group, blood sampling for baseline measurements was performed on the first day of hospital stay - before the commencement of treatment with ursodeoxycholic acid (UDCA) - and repeated after 7 days of 900 mg UDCA per day. An additional blood sample was collected on the second day after childbirth. In the control group, blood samples were collected directly after hospital admission. We compared plasma sphingolipids in samples of the subjects from ICP and ICP + UDCA-treated groups as well as the ICP group after delivery with the healthy controls.Of all sphingolipids, the median values of C16-Cer and C18-Cer were significantly higher in the plasma of cholestasis patients not treated with UDCA as compared to the control. Following 7 days of UDCA treatment, a considerable decrease in C16-Cer, C18-Cer and the total concentration of bile acids was noted as compared to the baseline.RESULTSOf all sphingolipids, the median values of C16-Cer and C18-Cer were significantly higher in the plasma of cholestasis patients not treated with UDCA as compared to the control. Following 7 days of UDCA treatment, a considerable decrease in C16-Cer, C18-Cer and the total concentration of bile acids was noted as compared to the baseline.It is known that sphingolipids serve as modulators of liver regeneration. We assume these substances could be potential markers for detecting early onsets of intrahepatic cholestasis of pregnancy.CONCLUSIONIt is known that sphingolipids serve as modulators of liver regeneration. We assume these substances could be potential markers for detecting early onsets of intrahepatic cholestasis of pregnancy.
•Intrahepatic cholestasis related perinatal complications include premature birth, meconium-stained amniotic fluid, fetal bradycardia, fetal respiratory distress syndrome and intrauterine fetal demise.•Cholestasis treatment with UDCA is known to be very effective.•Sphingolipids can potentially become screening markers as well as markers for monitoring the treatment of ICP in pregnant women. Intrahepatic cholestasis of pregnancy (ICP) is the most common pregnancy-related liver disorder that affects from 0.2% to 15.6% pregnant women. The disease is connected with increased risk of fetal morbidity and mortality, but is unfortunately detected quite late. The diagnosis of ICP is based on only one manifestation: pruritus which mainly affects soles and palms. Twenty intrahepatic cholestasis of pregnancy (ICP) women and twenty healthy pregnant women (control group) took part in the study. In the study group, blood sampling for baseline measurements was performed on the first day of hospital stay – before the commencement of treatment with ursodeoxycholic acid (UDCA) – and repeated after 7 days of 900 mg UDCA per day. An additional blood sample was collected on the second day after childbirth. In the control group, blood samples were collected directly after hospital admission. We compared plasma sphingolipids in samples of the subjects from ICP and ICP + UDCA-treated groups as well as the ICP group after delivery with the healthy controls. Of all sphingolipids, the median values of C16-Cer and C18-Cer were significantly higher in the plasma of cholestasis patients not treated with UDCA as compared to the control. Following 7 days of UDCA treatment, a considerable decrease in C16-Cer, C18-Cer and the total concentration of bile acids was noted as compared to the baseline. It is known that sphingolipids serve as modulators of liver regeneration. We assume these substances could be potential markers for detecting early onsets of intrahepatic cholestasis of pregnancy.
ArticleNumber 106399
Author Kacerovsky, Marian
Blachnio-Zabielska, Agnieszka
Kosinski, Przemyslaw
Mikucka-Niczyporuk, Agnieszka
Charkiewicz, Karol
Laudanski, Piotr
Knas, Małgorzata
Pierzynski, Piotr
Lemancewicz, Adam
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Cites_doi 10.1515/hsz-2014-0296
10.1097/AOG.0000000000000346
10.3390/ijms18122606
10.1371/journal.pone.0028343
10.1016/j.jhep.2009.04.009
10.1371/journal.pone.0127732
10.1111/liv.12331
10.1016/j.advms.2015.09.006
10.2478/v10039-009-0010-y
10.1194/jlr.R031278
10.1038/nature13475
10.1016/j.prostaglandins.2016.04.005
10.1111/j.1478-3231.2007.01475.x
10.1515/jpm-2014-0089
10.7326/0003-4819-88-4-487
10.1111/1471-0528.12174
10.1194/jlr.R800080-JLR200
10.1016/j.ajog.2014.07.026
10.1136/jmg.2004.026187
10.1002/hep.24193
10.1002/rcm.6216
10.1111/j.1478-3231.2011.02666.x
10.1038/nrc1411
10.1038/sj.jp.7211545
10.1007/s11010-010-0409-6
10.1515/jpm-2014-0207
10.1055/s-2008-1078756
10.1111/j.1872-034X.2011.00934.x
10.1016/S0140-6736(19)31607-1
10.1152/ajpendo.91014.2008
10.1089/jwh.2007.0158
10.1016/j.clinre.2015.12.008
10.3390/ijms18040741
10.2174/187152011797655140
10.1016/j.placenta.2016.07.002
10.1111/bcp.12480
10.1038/nri2400
10.1136/eb-2013-101298
10.1002/hep.20336
10.1016/S1388-1981(02)00341-4
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Keywords liver disorder
Sphingolipids
cholestasis
ceramides
Language English
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References Mari, Fernandez-Checa (bib0085) 2007; 27
Matsubara, Tanaka, Patterson, Cho, Krausz, Gonzalez (bib0090) 2011; 53
Kurek, Piotrowska, Wiesiołek-Kurek, Łukaszuk, Chabowski, Górski (bib0195) 2014; 34
Brouwers, Koster, Page-Christiaens, Kemperman, Boon, Evers (bib0005) 2015; 212
Young, Kester, Wang (bib0220) 2013; 54
Yang, Badeanlou, Bielawski, Roberts, Hannun, Samad (bib0200) 2009; 297
Stulic, Culafic, Boricic, Stojkovic Lalosevic, Pejic, Jankovic, Milovanovic, Culafic-Vojinovic, Vlaisavljevic, Culafic (bib0010) 2019; 55
Maceyka, Spiegel (bib0095) 2014; 510
Marschall (bib0125) 2019; 394
Rook, Vargas, Caughey, Bachetti, Rosenthal, Bull (bib0020) 2012; 7
European Association for the Study of the Liver (bib0055) 2009; 51
Glantz, Marschall, Mattsson (bib0060) 2004; 40
Wikström Shemer, Marschall, Ludvigsson, Stephansson (bib0120) 2013; 120
Carey, White (bib0130) 2013; 18
Ogretmen, Hannun (bib0165) 2004; 4
Oztas, Erkenekli, Ozler, Ersoy, Kurt, Oztas (bib0075) 2015; 43
Błachnio-Zabielska, Baranowski, Wójcik, Górski (bib0110) 2016; 61
Maceyka, Payne, Milstien, Spiegel (bib0180) 2002; 1585
Wollny, Wątek, Durnaś, Niemirowicz, Piktel, Żendzian-Piotrowska (bib0190) 2017; 18
Wierzbicki, Chabowski, Zendzian-Piotrowska, Harasim, Górski (bib0210) 2009; 54
Bao, Chen, Xu, Zhao, Zha, Huang (bib0155) 2012; 32
Reyes, Gonzales, Ribalta, Aburto, Matus, Schramm (bib0025) 1978; 88
Saleh, Abdo (bib0035) 2007; 16
Williamson, Geenes (bib0030) 2014; 124
Lee, Kwok, Ingles, Wilson, Mullin, Incerpi (bib0050) 2008; 25
Burns, Luberto (bib0160) 2011; 11
Konończuk, Łukaszuk, Żendzian-Piotrowska, Dąbrowski, Krzyżak, Ostrowska (bib0170) 2017; 18
Rivera, Proia, Olivera (bib0185) 2008; 8
Mella, Kohari, Jones, Pena, Ferrara, Stone (bib0065) 2016; 45
Laudanski, Charkiewicz, Kisielewski, Kuc, Koc-Zorawska, Raba (bib0225) 2016; 123
Bartke, Hannun (bib0175) 2009; 50
Dixon, Williamson (bib0070) 2016; 40
Blachnio-Zabielska, Persson, Koutsari, Zabielski, Jensen (bib0115) 2012; 26
Mil van, Houwen, Klomp (bib0150) 2005; 42
Knaś, Lukivskaya, Karaszewska, Borzym-Kluczyk, Dudzik, Zawadnik (bib0135) 2007; 3
Šimják, Pařízek, Vítek, Černý, Adamcová, Koucký (bib0040) 2015; 43
Puljic, Kim, Page, Esakoff, Shaffer, LaCoursiere (bib0015) 2015; 212
Goossens, Bailly (bib0145) 2019
Nojima, Freeman, Gulbins, Lentsch (bib0100) 2015; 396
Estiú, Monte, Rivas, Moirón, Gomez-Rodriguez, Rodriguez-Bravo (bib0140) 2015; 79
Chocian, Chabowski, Zendzian-Piotrowska, Harasim, Łukaszuk, Górski (bib0215) 2010; 340
Lee, Goodwin, Greenspoon, Incerpi (bib0045) 2006; 26
Charkiewicz, Blachnio-Zabielska, Zbucka-Kretowska, Wolczynski, Laudanski (bib0105) 2015; 10
Longato, Tong, Wands, de la Monte (bib0205) 2012; 42
Royal College of Obstetricians & Gynaecologists. Obstetric Cholestasis (bib0080) 2011
Stulic (10.1016/j.prostaglandins.2019.106399_bib0010) 2019; 55
Lee (10.1016/j.prostaglandins.2019.106399_bib0050) 2008; 25
Knaś (10.1016/j.prostaglandins.2019.106399_bib0135) 2007; 3
Rook (10.1016/j.prostaglandins.2019.106399_bib0020) 2012; 7
Williamson (10.1016/j.prostaglandins.2019.106399_bib0030) 2014; 124
Royal College of Obstetricians & Gynaecologists. Obstetric Cholestasis (10.1016/j.prostaglandins.2019.106399_bib0080) 2011
Estiú (10.1016/j.prostaglandins.2019.106399_bib0140) 2015; 79
Lee (10.1016/j.prostaglandins.2019.106399_bib0045) 2006; 26
Konończuk (10.1016/j.prostaglandins.2019.106399_bib0170) 2017; 18
Wierzbicki (10.1016/j.prostaglandins.2019.106399_bib0210) 2009; 54
Blachnio-Zabielska (10.1016/j.prostaglandins.2019.106399_bib0115) 2012; 26
Maceyka (10.1016/j.prostaglandins.2019.106399_bib0095) 2014; 510
Kurek (10.1016/j.prostaglandins.2019.106399_bib0195) 2014; 34
Maceyka (10.1016/j.prostaglandins.2019.106399_bib0180) 2002; 1585
Mari (10.1016/j.prostaglandins.2019.106399_bib0085) 2007; 27
Mella (10.1016/j.prostaglandins.2019.106399_bib0065) 2016; 45
Saleh (10.1016/j.prostaglandins.2019.106399_bib0035) 2007; 16
Bartke (10.1016/j.prostaglandins.2019.106399_bib0175) 2009; 50
Yang (10.1016/j.prostaglandins.2019.106399_bib0200) 2009; 297
Dixon (10.1016/j.prostaglandins.2019.106399_bib0070) 2016; 40
Wollny (10.1016/j.prostaglandins.2019.106399_bib0190) 2017; 18
Matsubara (10.1016/j.prostaglandins.2019.106399_bib0090) 2011; 53
Charkiewicz (10.1016/j.prostaglandins.2019.106399_bib0105) 2015; 10
Oztas (10.1016/j.prostaglandins.2019.106399_bib0075) 2015; 43
Reyes (10.1016/j.prostaglandins.2019.106399_bib0025) 1978; 88
Błachnio-Zabielska (10.1016/j.prostaglandins.2019.106399_bib0110) 2016; 61
Brouwers (10.1016/j.prostaglandins.2019.106399_bib0005) 2015; 212
Young (10.1016/j.prostaglandins.2019.106399_bib0220) 2013; 54
European Association for the Study of the Liver (10.1016/j.prostaglandins.2019.106399_bib0055) 2009; 51
Glantz (10.1016/j.prostaglandins.2019.106399_bib0060) 2004; 40
Wikström Shemer (10.1016/j.prostaglandins.2019.106399_bib0120) 2013; 120
Puljic (10.1016/j.prostaglandins.2019.106399_bib0015) 2015; 212
Rivera (10.1016/j.prostaglandins.2019.106399_bib0185) 2008; 8
Šimják (10.1016/j.prostaglandins.2019.106399_bib0040) 2015; 43
Laudanski (10.1016/j.prostaglandins.2019.106399_bib0225) 2016; 123
Ogretmen (10.1016/j.prostaglandins.2019.106399_bib0165) 2004; 4
Mil van (10.1016/j.prostaglandins.2019.106399_bib0150) 2005; 42
Nojima (10.1016/j.prostaglandins.2019.106399_bib0100) 2015; 396
Burns (10.1016/j.prostaglandins.2019.106399_bib0160) 2011; 11
Marschall (10.1016/j.prostaglandins.2019.106399_bib0125) 2019; 394
Longato (10.1016/j.prostaglandins.2019.106399_bib0205) 2012; 42
Carey (10.1016/j.prostaglandins.2019.106399_bib0130) 2013; 18
Goossens (10.1016/j.prostaglandins.2019.106399_bib0145) 2019
Bao (10.1016/j.prostaglandins.2019.106399_bib0155) 2012; 32
Chocian (10.1016/j.prostaglandins.2019.106399_bib0215) 2010; 340
References_xml – volume: 10
  start-page: e0127732
  year: 2015
  ident: bib0105
  article-title: Maternal plasma and amniotic fluid sphingolipids profiling in fetal Down syndrome
  publication-title: PLoS One
– volume: 8
  start-page: 753
  year: 2008
  end-page: 763
  ident: bib0185
  article-title: The alliance of sphingosine-1-phosphate and its receptors in immunity
  publication-title: Nat Rev Immunol
– volume: 18
  year: 2013
  ident: bib0130
  article-title: Ursodeoxycholic acid for intrahepatic cholestasis of pregnancy: good for the mother, not bad for the baby
  publication-title: Evid Based Med
– volume: 124
  start-page: 120
  year: 2014
  end-page: 133
  ident: bib0030
  article-title: Intrahepatic cholestasis of pregnancy
  publication-title: Obstet Gynecol
– volume: 297
  start-page: E211
  year: 2009
  end-page: 24
  ident: bib0200
  article-title: Central role of ceramide biosynthesis in body weight regulation, energy metabolism, and the metabolic syndrome
  publication-title: Am J Physiol Endocrinol Metab
– volume: 394
  start-page: 810
  year: 2019
  end-page: 812
  ident: bib0125
  article-title: Ursodeoxycholic acid for intrahepatic cholestasis in pregnancy
  publication-title: Lancet
– volume: 18
  start-page: E2606
  year: 2017
  ident: bib0170
  article-title: Plasma sphingolipids in acute pancreatitis
  publication-title: Int J Mol Sci
– year: 2011
  ident: bib0080
  article-title: Green-Top Guideline No. 43
– volume: 1585
  start-page: 193
  year: 2002
  end-page: 201
  ident: bib0180
  article-title: Sphingosine kinase, sphingosine-1-phosphate, and apoptosis
  publication-title: Biochim Biophys Acta
– volume: 54
  start-page: 59
  year: 2009
  end-page: 65
  ident: bib0210
  article-title: Chronic, in vivo, PPARalpha activation prevents lipid overload in rat liver induced by high fat feeding
  publication-title: Adv Med Sci
– volume: 212
  start-page: 667
  year: 2015
  ident: bib0015
  article-title: The risk of infant and fetal death by each additional week of expectant management in intrahepatic cholestasis of pregnancy by gestation age
  publication-title: Am J Obstet Gynecol
– volume: 61
  start-page: 72
  year: 2016
  end-page: 77
  ident: bib0110
  article-title: Reduction of ceramide de novo synthesis in solid tissues changes sphingolipid levels in rat plasma, erythrocytes and platelets
  publication-title: Adv Med Sci
– volume: 120
  start-page: 717
  year: 2013
  end-page: 723
  ident: bib0120
  article-title: Intrahepatic cholestasis of pregnancy and associated adverse pregnancy and fetal outcomes: a 12-year population-based cohort study
  publication-title: BJOG
– volume: 25
  start-page: 341
  year: 2008
  end-page: 345
  ident: bib0050
  article-title: Pregnancy outcomes Turing an era of aggressive management for intrahepatic cholestasis of pregnancy
  publication-title: Am J Perinatol
– volume: 45
  start-page: 16
  year: 2016
  end-page: 23
  ident: bib0065
  article-title: Mitochondrial gene expression profiles are associated with intrahepatic cholestasis of pregnancy
  publication-title: Placenta
– volume: 88
  start-page: 487
  year: 1978
  end-page: 493
  ident: bib0025
  article-title: Prevalence of intrahepatic cholestasis of pregnancy in Chile
  publication-title: Ann Intern Med
– volume: 32
  start-page: 331
  year: 2012
  end-page: 338
  ident: bib0155
  article-title: Sphingosine kinase 1 promotes tumour cell migration and invasion via the S1P/EDG1 axis in hepatocellular carcinoma
  publication-title: Liver Int
– volume: 42
  start-page: 412
  year: 2012
  end-page: 427
  ident: bib0205
  article-title: High fat diet induced hepatic steatosis and insulin resistance: role of dysregulated ceramide metabolism
  publication-title: Hepatol Res
– volume: 27
  start-page: 440
  year: 2007
  end-page: 450
  ident: bib0085
  article-title: Sphingolipid signalling and liver diseases
  publication-title: Liver Int
– volume: 7
  start-page: e28343
  year: 2012
  ident: bib0020
  article-title: Fetal outcomes in pregnancy complicated by intrahepatic cholestasis of pregnancy in a Northern California cohort
  publication-title: PLoS One
– volume: 11
  start-page: 863
  year: 2011
  end-page: 881
  ident: bib0160
  article-title: Sphingolipid metabolism and leukemia: A potential for novel therapeutic approaches
  publication-title: Anticancer Agents Med Chem
– volume: 34
  start-page: 1074
  year: 2014
  end-page: 1083
  ident: bib0195
  article-title: Inhibition of ceramide de novo synthesis reduces liver lipid accumulation in rats with nonalcoholic fatty liver disease
  publication-title: Liver Int
– volume: 3
  start-page: 21
  year: 2007
  end-page: 24
  ident: bib0135
  article-title: UDCA and activity of exoglycosidases in liver, kidney and serum of stressed rats
  publication-title: ExpClin Hepatology
– volume: 123
  start-page: 40
  year: 2016
  end-page: 45
  ident: bib0225
  article-title: Plasma C16-Cer levels are increase in patients with preterm labor
  publication-title: Prostaglandins Other Lipid Mediat
– volume: 51
  start-page: 237
  year: 2009
  end-page: 267
  ident: bib0055
  article-title: EASL Clinical Practice Guidelines: Management of cholestatic liver diseases
  publication-title: J Hepatol
– volume: 79
  start-page: 316
  year: 2015
  end-page: 329
  ident: bib0140
  article-title: Effect of ursodeoxycholic acid treatment on the altered progesterone and bile acid homeostasis in the mother-placenta-foetus trio during cholestasis of pregnancy
  publication-title: Br J Clin Pharmacol
– volume: 42
  start-page: 449
  year: 2005
  end-page: 463
  ident: bib0150
  article-title: Genetics of familial intrahepatic cholestasis syndromes
  publication-title: J Med Genet
– volume: 26
  start-page: 1134
  year: 2012
  end-page: 1140
  ident: bib0115
  article-title: A liquid chromatography/tandem mass spectrometry method for measuring the in vivo incorporation of plasma free fatty acids into intramyocellular ceramides in humans
  publication-title: Rapid Commun Mass Spectrom
– volume: 4
  start-page: 604
  year: 2004
  end-page: 616
  ident: bib0165
  article-title: Biologically active sphingolipids in cancer pathogenesis and treatment
  publication-title: Nat Rev Cancer
– volume: 396
  start-page: 633
  year: 2015
  end-page: 643
  ident: bib0100
  article-title: Sphingolipids in liver injury, repair and regeneration
  publication-title: Biol Chem
– volume: 50
  start-page: S91
  year: 2009
  end-page: S96
  ident: bib0175
  article-title: Bioactive sphingolipids: Metabolism and function
  publication-title: J Lipid Res
– volume: 54
  start-page: 5
  year: 2013
  end-page: 19
  ident: bib0220
  article-title: Sphingolipids: regulators of cross talk between apoptosis and autophagy
  publication-title: J Lipid Res
– year: 2019
  ident: bib0145
  article-title: Ursodeoxycholic acid and cancer: From chemoprevention to chemotherapy
  publication-title: Pharmacol Ther.
– volume: 40
  start-page: 467
  year: 2004
  end-page: 474
  ident: bib0060
  article-title: Intrahepatic cholestasis of pregnancy: Relationship between bile acid levels and fetal complication rates
  publication-title: Hepatology
– volume: 55
  year: 2019
  ident: bib0010
  article-title: Intrahepatic Cholestasis of Pregnancy: A Case Study of the Rare Onset in the First Trimester
  publication-title: Medicina (Kaunas)
– volume: 18
  start-page: E741
  year: 2017
  ident: bib0190
  article-title: Sphingosine-1-phosphate metabolism and its role in the development of inflammatory bowel disease
  publication-title: Int J Mol Sci
– volume: 212
  start-page: 100
  year: 2015
  ident: bib0005
  article-title: Intrahepatic cholestasis of pregnancy: maternal and fetal outcomes associated with elevated bile acid levels
  publication-title: Am J Obstet Gynecol
– volume: 43
  start-page: 133
  year: 2015
  end-page: 139
  ident: bib0040
  article-title: Fetal complications due to intrahepatic cholestasis of pregnancy
  publication-title: J Perinat Med
– volume: 43
  start-page: 667
  year: 2015
  end-page: 674
  ident: bib0075
  article-title: Can routine laboratory parameters predict adverse pregnancy outcomes in intrahepatic cholestasis of pregnancy?
  publication-title: J Perinat Med
– volume: 340
  start-page: 125
  year: 2010
  end-page: 131
  ident: bib0215
  article-title: High fat diet induces ceramide and sphingomyelin formation in rat’s liver nuclei
  publication-title: Mol Cell Biochem
– volume: 53
  start-page: 1282
  year: 2011
  end-page: 1293
  ident: bib0090
  article-title: Lithocholic acid disrupts phospholipid and sphingolipid homeostasis leading to cholestasis in mice
  publication-title: Hepatology
– volume: 26
  start-page: 527
  year: 2006
  end-page: 532
  ident: bib0045
  article-title: The prevalence of intrahepatic cholestasis of pregnancy in a primarily Latina Los Angeles population
  publication-title: J Perinatol
– volume: 40
  start-page: 141
  year: 2016
  end-page: 153
  ident: bib0070
  article-title: The pathophysiology of intrahepatic cholestasis of pregnancy
  publication-title: Clin Res Hepatol Gastroenterol.
– volume: 16
  start-page: 833
  year: 2007
  end-page: 841
  ident: bib0035
  article-title: Intrahepatic cholestasis of pregnancy: review of the literature and evaluation of current evidence
  publication-title: J Womens Health
– volume: 510
  start-page: 58
  year: 2014
  end-page: 67
  ident: bib0095
  article-title: Sphingolipid metabolites in inflammatory disease
  publication-title: Nature
– volume: 396
  start-page: 633
  year: 2015
  ident: 10.1016/j.prostaglandins.2019.106399_bib0100
  article-title: Sphingolipids in liver injury, repair and regeneration
  publication-title: Biol Chem
  doi: 10.1515/hsz-2014-0296
– volume: 124
  start-page: 120
  year: 2014
  ident: 10.1016/j.prostaglandins.2019.106399_bib0030
  article-title: Intrahepatic cholestasis of pregnancy
  publication-title: Obstet Gynecol
  doi: 10.1097/AOG.0000000000000346
– volume: 18
  start-page: E2606
  year: 2017
  ident: 10.1016/j.prostaglandins.2019.106399_bib0170
  article-title: Plasma sphingolipids in acute pancreatitis
  publication-title: Int J Mol Sci
  doi: 10.3390/ijms18122606
– volume: 7
  start-page: e28343
  year: 2012
  ident: 10.1016/j.prostaglandins.2019.106399_bib0020
  article-title: Fetal outcomes in pregnancy complicated by intrahepatic cholestasis of pregnancy in a Northern California cohort
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0028343
– volume: 51
  start-page: 237
  year: 2009
  ident: 10.1016/j.prostaglandins.2019.106399_bib0055
  article-title: EASL Clinical Practice Guidelines: Management of cholestatic liver diseases
  publication-title: J Hepatol
  doi: 10.1016/j.jhep.2009.04.009
– volume: 10
  start-page: e0127732
  year: 2015
  ident: 10.1016/j.prostaglandins.2019.106399_bib0105
  article-title: Maternal plasma and amniotic fluid sphingolipids profiling in fetal Down syndrome
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0127732
– volume: 34
  start-page: 1074
  year: 2014
  ident: 10.1016/j.prostaglandins.2019.106399_bib0195
  article-title: Inhibition of ceramide de novo synthesis reduces liver lipid accumulation in rats with nonalcoholic fatty liver disease
  publication-title: Liver Int
  doi: 10.1111/liv.12331
– volume: 61
  start-page: 72
  year: 2016
  ident: 10.1016/j.prostaglandins.2019.106399_bib0110
  article-title: Reduction of ceramide de novo synthesis in solid tissues changes sphingolipid levels in rat plasma, erythrocytes and platelets
  publication-title: Adv Med Sci
  doi: 10.1016/j.advms.2015.09.006
– volume: 54
  start-page: 59
  year: 2009
  ident: 10.1016/j.prostaglandins.2019.106399_bib0210
  article-title: Chronic, in vivo, PPARalpha activation prevents lipid overload in rat liver induced by high fat feeding
  publication-title: Adv Med Sci
  doi: 10.2478/v10039-009-0010-y
– volume: 54
  start-page: 5
  year: 2013
  ident: 10.1016/j.prostaglandins.2019.106399_bib0220
  article-title: Sphingolipids: regulators of cross talk between apoptosis and autophagy
  publication-title: J Lipid Res
  doi: 10.1194/jlr.R031278
– volume: 510
  start-page: 58
  year: 2014
  ident: 10.1016/j.prostaglandins.2019.106399_bib0095
  article-title: Sphingolipid metabolites in inflammatory disease
  publication-title: Nature
  doi: 10.1038/nature13475
– volume: 3
  start-page: 21
  year: 2007
  ident: 10.1016/j.prostaglandins.2019.106399_bib0135
  article-title: UDCA and activity of exoglycosidases in liver, kidney and serum of stressed rats
  publication-title: ExpClin Hepatology
– volume: 123
  start-page: 40
  year: 2016
  ident: 10.1016/j.prostaglandins.2019.106399_bib0225
  article-title: Plasma C16-Cer levels are increase in patients with preterm labor
  publication-title: Prostaglandins Other Lipid Mediat
  doi: 10.1016/j.prostaglandins.2016.04.005
– volume: 27
  start-page: 440
  year: 2007
  ident: 10.1016/j.prostaglandins.2019.106399_bib0085
  article-title: Sphingolipid signalling and liver diseases
  publication-title: Liver Int
  doi: 10.1111/j.1478-3231.2007.01475.x
– issue: July
  year: 2019
  ident: 10.1016/j.prostaglandins.2019.106399_bib0145
  article-title: Ursodeoxycholic acid and cancer: From chemoprevention to chemotherapy
  publication-title: Pharmacol Ther.
– volume: 43
  start-page: 133
  year: 2015
  ident: 10.1016/j.prostaglandins.2019.106399_bib0040
  article-title: Fetal complications due to intrahepatic cholestasis of pregnancy
  publication-title: J Perinat Med
  doi: 10.1515/jpm-2014-0089
– volume: 88
  start-page: 487
  year: 1978
  ident: 10.1016/j.prostaglandins.2019.106399_bib0025
  article-title: Prevalence of intrahepatic cholestasis of pregnancy in Chile
  publication-title: Ann Intern Med
  doi: 10.7326/0003-4819-88-4-487
– volume: 120
  start-page: 717
  year: 2013
  ident: 10.1016/j.prostaglandins.2019.106399_bib0120
  article-title: Intrahepatic cholestasis of pregnancy and associated adverse pregnancy and fetal outcomes: a 12-year population-based cohort study
  publication-title: BJOG
  doi: 10.1111/1471-0528.12174
– volume: 50
  start-page: S91
  year: 2009
  ident: 10.1016/j.prostaglandins.2019.106399_bib0175
  article-title: Bioactive sphingolipids: Metabolism and function
  publication-title: J Lipid Res
  doi: 10.1194/jlr.R800080-JLR200
– volume: 212
  start-page: 100
  year: 2015
  ident: 10.1016/j.prostaglandins.2019.106399_bib0005
  article-title: Intrahepatic cholestasis of pregnancy: maternal and fetal outcomes associated with elevated bile acid levels
  publication-title: Am J Obstet Gynecol
  doi: 10.1016/j.ajog.2014.07.026
– volume: 42
  start-page: 449
  year: 2005
  ident: 10.1016/j.prostaglandins.2019.106399_bib0150
  article-title: Genetics of familial intrahepatic cholestasis syndromes
  publication-title: J Med Genet
  doi: 10.1136/jmg.2004.026187
– volume: 53
  start-page: 1282
  year: 2011
  ident: 10.1016/j.prostaglandins.2019.106399_bib0090
  article-title: Lithocholic acid disrupts phospholipid and sphingolipid homeostasis leading to cholestasis in mice
  publication-title: Hepatology
  doi: 10.1002/hep.24193
– volume: 26
  start-page: 1134
  year: 2012
  ident: 10.1016/j.prostaglandins.2019.106399_bib0115
  article-title: A liquid chromatography/tandem mass spectrometry method for measuring the in vivo incorporation of plasma free fatty acids into intramyocellular ceramides in humans
  publication-title: Rapid Commun Mass Spectrom
  doi: 10.1002/rcm.6216
– volume: 32
  start-page: 331
  year: 2012
  ident: 10.1016/j.prostaglandins.2019.106399_bib0155
  article-title: Sphingosine kinase 1 promotes tumour cell migration and invasion via the S1P/EDG1 axis in hepatocellular carcinoma
  publication-title: Liver Int
  doi: 10.1111/j.1478-3231.2011.02666.x
– year: 2011
  ident: 10.1016/j.prostaglandins.2019.106399_bib0080
– volume: 4
  start-page: 604
  year: 2004
  ident: 10.1016/j.prostaglandins.2019.106399_bib0165
  article-title: Biologically active sphingolipids in cancer pathogenesis and treatment
  publication-title: Nat Rev Cancer
  doi: 10.1038/nrc1411
– volume: 26
  start-page: 527
  year: 2006
  ident: 10.1016/j.prostaglandins.2019.106399_bib0045
  article-title: The prevalence of intrahepatic cholestasis of pregnancy in a primarily Latina Los Angeles population
  publication-title: J Perinatol
  doi: 10.1038/sj.jp.7211545
– volume: 340
  start-page: 125
  year: 2010
  ident: 10.1016/j.prostaglandins.2019.106399_bib0215
  article-title: High fat diet induces ceramide and sphingomyelin formation in rat’s liver nuclei
  publication-title: Mol Cell Biochem
  doi: 10.1007/s11010-010-0409-6
– volume: 43
  start-page: 667
  year: 2015
  ident: 10.1016/j.prostaglandins.2019.106399_bib0075
  article-title: Can routine laboratory parameters predict adverse pregnancy outcomes in intrahepatic cholestasis of pregnancy?
  publication-title: J Perinat Med
  doi: 10.1515/jpm-2014-0207
– volume: 25
  start-page: 341
  year: 2008
  ident: 10.1016/j.prostaglandins.2019.106399_bib0050
  article-title: Pregnancy outcomes Turing an era of aggressive management for intrahepatic cholestasis of pregnancy
  publication-title: Am J Perinatol
  doi: 10.1055/s-2008-1078756
– volume: 42
  start-page: 412
  year: 2012
  ident: 10.1016/j.prostaglandins.2019.106399_bib0205
  article-title: High fat diet induced hepatic steatosis and insulin resistance: role of dysregulated ceramide metabolism
  publication-title: Hepatol Res
  doi: 10.1111/j.1872-034X.2011.00934.x
– volume: 394
  start-page: 810
  issue: 10201
  year: 2019
  ident: 10.1016/j.prostaglandins.2019.106399_bib0125
  article-title: Ursodeoxycholic acid for intrahepatic cholestasis in pregnancy
  publication-title: Lancet
  doi: 10.1016/S0140-6736(19)31607-1
– volume: 55
  issue: August (8)
  year: 2019
  ident: 10.1016/j.prostaglandins.2019.106399_bib0010
  article-title: Intrahepatic Cholestasis of Pregnancy: A Case Study of the Rare Onset in the First Trimester
  publication-title: Medicina (Kaunas)
– volume: 212
  start-page: 667
  year: 2015
  ident: 10.1016/j.prostaglandins.2019.106399_bib0015
  article-title: The risk of infant and fetal death by each additional week of expectant management in intrahepatic cholestasis of pregnancy by gestation age
  publication-title: Am J Obstet Gynecol
– volume: 297
  start-page: E211
  year: 2009
  ident: 10.1016/j.prostaglandins.2019.106399_bib0200
  article-title: Central role of ceramide biosynthesis in body weight regulation, energy metabolism, and the metabolic syndrome
  publication-title: Am J Physiol Endocrinol Metab
  doi: 10.1152/ajpendo.91014.2008
– volume: 16
  start-page: 833
  year: 2007
  ident: 10.1016/j.prostaglandins.2019.106399_bib0035
  article-title: Intrahepatic cholestasis of pregnancy: review of the literature and evaluation of current evidence
  publication-title: J Womens Health
  doi: 10.1089/jwh.2007.0158
– volume: 40
  start-page: 141
  issue: April (2)
  year: 2016
  ident: 10.1016/j.prostaglandins.2019.106399_bib0070
  article-title: The pathophysiology of intrahepatic cholestasis of pregnancy
  publication-title: Clin Res Hepatol Gastroenterol.
  doi: 10.1016/j.clinre.2015.12.008
– volume: 18
  start-page: E741
  year: 2017
  ident: 10.1016/j.prostaglandins.2019.106399_bib0190
  article-title: Sphingosine-1-phosphate metabolism and its role in the development of inflammatory bowel disease
  publication-title: Int J Mol Sci
  doi: 10.3390/ijms18040741
– volume: 11
  start-page: 863
  year: 2011
  ident: 10.1016/j.prostaglandins.2019.106399_bib0160
  article-title: Sphingolipid metabolism and leukemia: A potential for novel therapeutic approaches
  publication-title: Anticancer Agents Med Chem
  doi: 10.2174/187152011797655140
– volume: 45
  start-page: 16
  year: 2016
  ident: 10.1016/j.prostaglandins.2019.106399_bib0065
  article-title: Mitochondrial gene expression profiles are associated with intrahepatic cholestasis of pregnancy
  publication-title: Placenta
  doi: 10.1016/j.placenta.2016.07.002
– volume: 79
  start-page: 316
  year: 2015
  ident: 10.1016/j.prostaglandins.2019.106399_bib0140
  article-title: Effect of ursodeoxycholic acid treatment on the altered progesterone and bile acid homeostasis in the mother-placenta-foetus trio during cholestasis of pregnancy
  publication-title: Br J Clin Pharmacol
  doi: 10.1111/bcp.12480
– volume: 8
  start-page: 753
  year: 2008
  ident: 10.1016/j.prostaglandins.2019.106399_bib0185
  article-title: The alliance of sphingosine-1-phosphate and its receptors in immunity
  publication-title: Nat Rev Immunol
  doi: 10.1038/nri2400
– volume: 18
  year: 2013
  ident: 10.1016/j.prostaglandins.2019.106399_bib0130
  article-title: Ursodeoxycholic acid for intrahepatic cholestasis of pregnancy: good for the mother, not bad for the baby
  publication-title: Evid Based Med
  doi: 10.1136/eb-2013-101298
– volume: 40
  start-page: 467
  year: 2004
  ident: 10.1016/j.prostaglandins.2019.106399_bib0060
  article-title: Intrahepatic cholestasis of pregnancy: Relationship between bile acid levels and fetal complication rates
  publication-title: Hepatology
  doi: 10.1002/hep.20336
– volume: 1585
  start-page: 193
  year: 2002
  ident: 10.1016/j.prostaglandins.2019.106399_bib0180
  article-title: Sphingosine kinase, sphingosine-1-phosphate, and apoptosis
  publication-title: Biochim Biophys Acta
  doi: 10.1016/S1388-1981(02)00341-4
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Snippet •Intrahepatic cholestasis related perinatal complications include premature birth, meconium-stained amniotic fluid, fetal bradycardia, fetal respiratory...
Intrahepatic cholestasis of pregnancy (ICP) is the most common pregnancy-related liver disorder that affects from 0.2% to 15.6% pregnant women. The disease is...
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SubjectTerms Adult
Bile Acids and Salts - blood
Biomarkers - blood
Case-Control Studies
ceramides
Cholagogues and Choleretics - therapeutic use
cholestasis
Cholestasis, Intrahepatic - blood
Cholestasis, Intrahepatic - drug therapy
Cholestasis, Intrahepatic - pathology
Female
Fetus - abnormalities
Humans
liver disorder
Pregnancy
Pregnancy Complications - blood
Pregnancy Complications - drug therapy
Pregnancy Complications - pathology
Sphingolipids
Sphingolipids - blood
Ursodeoxycholic Acid - therapeutic use
Title Role of sphingolipids in the pathogenesis of intrahepatic cholestasis
URI https://dx.doi.org/10.1016/j.prostaglandins.2019.106399
https://www.ncbi.nlm.nih.gov/pubmed/31733339
https://www.proquest.com/docview/2315082751
Volume 147
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